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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 31344생성일: 2026년 10월 23일

Tetrahydrofuran → 5-Chloro-3-hydroxy-3-(3-methoxyphenyl)-1,3-dihydro-2H-indol-2-one

https://huagongshe.com/ko/reaction/31344

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물3-BromoanisoleHCID 16971—
반응물Ammonium ChlorideHCID 25517—
반응물5-chloro-1H-indole-2,3-dioneHCID 87203—
반응물MagnesiumHCID 5462224—
생성물5-Chloro-3-hydroxy-3-(3-methoxyphenyl)-1,3-dihydro-2H-indol-2-oneHCID 22560825—
생성물HCID 178490745HCID 178490745—

반응 단계

A solution of 3-methoxyphenylmagnesium bromide is prepared from 3.5 g of magnesium in 10 ml of THF and from a solution of 25 g of 1-bromo-3-methoxy-benzene in 40 ml of THF. This solution is added dropwise, under a nitrogen atmosphere, to a mixture of 8 g of 5-chloro-1H-indole-2,3-dione in 50 ml of THF, while keeping the temperature of the reaction medium below 40° C., followed by refluxing for 1 hour. The reaction mixture is cooled to RT, poured into saturated NH4Cl solution and extracted with EtOAc, the organic phase is washed with water and dried over Na2SO4, and the solvent is evaporated off under vacuum. 9.1 g of the expected product are obtained after crystallization from hot iso ether; m.p.=212° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07425566B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-1935a5b414384453ae3b0fd32dff8349
출처 메모uspto-grants-2008_09